Neutrophil specific granule and NETosis defects in gray platelet syndrome

Gray platelet syndrome (GPS) is an autosomal recessive bleeding disorder characterized by a lack of α-granules in platelets and progressive myelofibrosis. Rare loss-of-function variants in neurobeachin-like 2 (NBEAL2), a member of the family of beige and Chédiak-Higashi (BEACH) genes, are causal of...

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Detalhes bibliográficos
Publicado no:Blood Adv
Main Authors: Aarts, Cathelijn E. M., Downes, Kate, Hoogendijk, Arie J., Sprenkeler, Evelien G. G., Gazendam, Roel P., Favier, Rémi, Favier, Marie, Tool, Anton T. J., van Hamme, John L., Kostadima, Myrto A., Waller, Kate, Zieger, Barbara, van Bergen, Maaike G. J. M., Langemeijer, Saskia M. C., van der Reijden, Bert A., Janssen, Hans, van den Berg, Timo K., van Bruggen, Robin, Meijer, Alexander B., Ouwehand, Willem H., Kuijpers, Taco W.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2021
Assuntos:
Phagocytes, Granulocytes, and Myelopoiesis
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7839360/
https://ncbi.nlm.nih.gov/pubmed/33496751
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2020002442
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